Canonical Allele Identifier: CA364418961

Gene: PKHD1

Linked Data

• MyVariant Identifiers: chr6:g.51491899T>A (hg19) ; chr6:g.51627101T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.51627101T>A , CM000668.2:g.51627101T>A	GRCh38
NC_000006.11:g.51491899T>A , CM000668.1:g.51491899T>A	GRCh37
NC_000006.10:g.51599858T>A	NCBI36
NG_008753.1:g.465525A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371117.8:c.11681A>T MANE Select	ENSP00000360158.3:p.Glu3894Val
ENST00000371117.7:c.11681A>T	ENSP00000360158.3:p.Glu3894Val
NM_138694.3:c.11681A>T	NP_619639.3:p.Glu3894Val
XM_011514679.1:c.11681A>T	XP_011512981.1:p.Glu3894Val
XM_011514680.1:c.11681A>T	XP_011512982.1:p.Glu3894Val
XM_011514681.1:c.11552A>T	XP_011512983.1:p.Glu3851Val
XM_011514682.1:c.11543A>T	XP_011512984.1:p.Glu3848Val
XM_011514683.1:c.11039A>T	XP_011512985.1:p.Glu3680Val
XM_011514684.1:c.10970A>T	XP_011512986.1:p.Glu3657Val
XM_011514690.1:c.5756A>T	XP_011512992.1:p.Glu1919Val
XM_011514691.1:c.5756A>T	XP_011512993.1:p.Glu1919Val
XM_011514680.3:c.11681A>T	XP_011512982.1:p.Glu3894Val
XM_011514682.3:c.11543A>T	XP_011512984.1:p.Glu3848Val
XM_011514683.3:c.11039A>T	XP_011512985.1:p.Glu3680Val
XM_011514684.3:c.10970A>T	XP_011512986.1:p.Glu3657Val
XM_011514690.3:c.5756A>T	XP_011512992.1:p.Glu1919Val
XM_011514691.3:c.5756A>T	XP_011512993.1:p.Glu1919Val
XM_017010944.2:c.11681A>T	XP_016866433.1:p.Glu3894Val
XM_017010945.2:c.11606A>T	XP_016866434.1:p.Glu3869Val
XM_017010946.2:c.11486A>T	XP_016866435.1:p.Glu3829Val
XM_017010947.2:c.11417A>T	XP_016866436.1:p.Glu3806Val
XM_017010948.2:c.10970A>T	XP_016866437.1:p.Glu3657Val
XM_017010949.2:c.9821A>T	XP_016866438.1:p.Glu3274Val
NM_138694.4:c.11681A>T MANE Select	NP_619639.3:p.Glu3894Val